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FDA 510(k)

Nexus DR Digital X-ray Imaging System

K-Number: K171138 · 2017-05-17

Decision Date2017-05-17
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Nexus DR Digital X-ray Imaging System is a medical device manufactured by Varex Imaging Corporation. It received FDA 510(k) clearance on 2017-05-17 under approval number K171138. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Nexus DR Digital X-ray Imaging System?

Nexus DR Digital X-ray Imaging System is a medical device that received FDA 510(k) clearance on 2017-05-17. It is manufactured by Varex Imaging Corporation. The 510(k) number is K171138.

When was Nexus DR Digital X-ray Imaging System approved by the FDA?

Nexus DR Digital X-ray Imaging System received FDA 510(k) clearance on 2017-05-17, under approval number K171138.

What company makes Nexus DR Digital X-ray Imaging System?

Nexus DR Digital X-ray Imaging System is manufactured by Varex Imaging Corporation.

What is the FDA product code for Nexus DR Digital X-ray Imaging System?

The FDA product code for Nexus DR Digital X-ray Imaging System is MQB.

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Official Source

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